Canonical Allele Identifier: CA2631551312

Gene: ROGDI

Linked Data

• gnomAD v4: 16-4798322-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.4798324del , CM000678.2:g.4798324del	GRCh38
NC_000016.9:g.4848325del , CM000678.1:g.4848325del	GRCh37
NC_000016.8:g.4788326del	NCBI36
NG_032174.1:g.9628del , LRG_455:g.9628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322048.12:c.532-139del MANE Select	ENSP00000322832.6:n.532-139del
ENST00000322048.11:c.532-139del	ENSP00000322832.5:n.532-139del
ENST00000586153.1:c.178-139del	ENSP00000464699.1:n.178-139del
ENST00000586336.5:n.631-139del
ENST00000586504.5:c.312-139del
ENST00000587377.5:c.545-139del	ENSP00000468343.1:n.545-139del
ENST00000587711.5:c.217-139del	ENSP00000467459.1:n.217-139del
ENST00000587843.5:c.*270-139del	ENSP00000465970.1:n.*270-139del
ENST00000588201.5:c.*523-139del	ENSP00000466529.1:n.*523-139del
ENST00000589543.5:n.489-139del
ENST00000591292.5:n.1861-139del
ENST00000591392.5:c.460-139del	ENSP00000467509.1:n.460-139del
ENST00000592019.1:c.77-508del
NM_024589.2:c.532-139del , LRG_455t1:c.532-139del	NP_078865.1:n.532-139del
NR_046480.1:n.856-139del
XM_006720947.2:c.532-139del	XP_006721010.1:n.532-139del
XM_006720948.2:c.262-139del	XP_006721011.1:n.262-139del
XM_006720947.4:c.532-139del	XP_006721010.1:n.532-139del
XM_006720948.4:c.262-139del	XP_006721011.1:n.262-139del
NM_024589.3:c.532-139del MANE Select	NP_078865.1:n.532-139del
NR_046480.2:n.539-139del